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SPIN CHEM REAGENT, DETERMINATION OF LDH-

K791081 Class II Traditional
Decision Date
1979-07-17
Sponsor / Applicant
Smithkline Diagnostics, Inc.

Technical Specification

510(k) Submission ID K791081
Product Code CFJ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1440
Decision Date 1979-07-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPIN CHEM REAGENT, DETERMINATION OF LDH- received FDA 510(k) clearance under submission number K791081, sponsored by Smithkline Diagnostics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1979-07-17.

Classification & Regulation

This clearance is catalogued under FDA product code CFJ and 21 CFR 862.1440, within the Clinical Chemistry review panel as a Class II device.